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ACOX1 antibody (AA 7-37)

This Rabbit Polyclonal antibody specifically detects ACOX1 in IHC and ELISA. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7479759
$612.54
Plus shipping costs $50.00
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Quick Overview for ACOX1 antibody (AA 7-37) (ABIN7479759)

Target

See all ACOX1 Antibodies
ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))

Reactivity

  • 69
  • 32
  • 15
Human, Mouse

Host

  • 63
  • 7
Rabbit

Clonality

  • 47
  • 23
Polyclonal

Conjugate

  • 35
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This ACOX1 antibody is un-conjugated

Application

  • 53
  • 34
  • 24
  • 17
  • 9
  • 4
  • 3
  • 2
Immunohistochemistry (IHC), ELISA
  • Binding Specificity

    • 8
    • 7
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 7-37

    Purpose

    ACOX1 Antibody / Peroxisomal acyl-coenzyme A oxidase 1

    Purification

    Purified

    Immunogen

    A portion of amino acids 7-37 from the human protein was used as the immunogen for this ACOX1 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the ACOX1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Aliquot the ACOX1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • Target

    ACOX1 (Acyl-CoA Oxidase 1, Palmitoyl (ACOX1))

    Alternative Name

    ACOX1

    Background

    ACOX1 is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids.

    UniProt

    Q15067

    Pathways

    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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